Linked Data
dbSNP Id:
rs774387819
ExAC:
21:35742733 C / A
gnomAD v2:
21-35742733-C-A
gnomAD v4:
21-34370434-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.34370434C>A , CM000683.2:g.34370434C>A | GRCh38 |
| NC_000021.8:g.35742733C>A , CM000683.1:g.35742733C>A | GRCh37 |
| NC_000021.7:g.34664603C>A | NCBI36 |
| NG_008804.1:g.11411C>A , LRG_291:g.11411C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000290310.4:c.-12-33C>A MANE Select | ENSP00000290310.2:n.-12-33C>A | |
| ENST00000290310.3:c.-12-33C>A | ENSP00000290310.2:n.-12-33C>A | |
| NM_172201.1:c.-12-33C>A , LRG_291t1:c.-12-33C>A | NP_751951.1:n.-12-33C>A | |
| XR_937683.1:n.886+1G>T | ||
| XR_937684.1:n.886+1G>T | ||
| XR_001755012.2:n.1008G>T | ||
| XR_001755013.2:n.887G>T | ||
| XR_937683.2:n.886+1G>T | ||
| NM_172201.2:c.-12-33C>A MANE Select | NP_751951.1:n.-12-33C>A |